G. Black

发表

Jeroen B. Klevering, C. Hoyng, P. Sergouniotis, 2020, Journal of Medical Genetics.

Alexander Klistorner, Bernhard Hemmer, Pablo Villoslada, 2017, The Lancet Neurology.

David L. Bennett, Kenneth G. C. Smith, Katherine R. Smith, 2019, Science.

K E Chandler, J. Clayton-Smith, L. Al-Gazali, 2003, Journal of medical genetics.

Rachel L. Taylor, E. Lenassi, S. Douzgou, 2019, European Journal of Human Genetics.

Kenneth G. C. Smith, Katherine R. Smith, K. Stirrups, 2019 .

J. Clayton-Smith, S. Smithson, F. Munier, 2013, Orphanet Journal of Rare Diseases.

Alexander M Phillips, P. Sergouniotis, Simon J. Clark, 2022, Proceedings of the National Academy of Sciences of the United States of America.

Rachel L. Taylor, C. Rivolta, D. Donnelly, 2020, Human mutation.

Rachel L. Taylor, J. Clayton-Smith, G. Hall, 2019, Genetics in Medicine.

P. Sergouniotis, N. Parry, K. Chandler, 2022, Acta ophthalmologica.

I. C. Lloyd, J. Clayton-Smith, S. Bhaskar, 2014, Ophthalmology.

G. Hall, G. Black, J. Ashworth, 2016, BMJ quality improvement reports.

G. Hall, K. Payne, A. Moore, 2013, British Journal of Ophthalmology.

P. Sergouniotis, G. Black, Sofia Douzgou Houge, 2022, Clinical Ophthalmic Genetics and Genomics.

R. Body, C. Morton, W. Newman, 2019, Trends in hearing.

Jennifer R. Davies, I. C. Lloyd, M. Votruba, 2014, neurogenetics.

Jeffrey N. Dudley, R. Holt, A. Schäffer, 2019, Journal of Medical Genetics.

Keith W. Muir, William J. Astle, Mark I. McCarthy, 2020, Nature.

Georgina Hall, Christopher Campbell, Rachel L. Taylor, 2017, Ophthalmology.

Robert A Hegele, Henian Cao, R. Hegele, 2007, Orphanet journal of rare diseases.

B. Lam, B. Leroy, G. Black, 2021, Orphanet Journal of Rare Diseases.

Kathryn E. Hentges, Matthieu J. Miossec, G. Lathrop, 2019, Circulation research.

D. Bonthron, F. Alkuraya, S. Bhaskar, 2013, Human mutation.

Binay Panda, Christopher Campbell, Saurabh Gupta, 2017, European Journal of Human Genetics.

Peter M. G. Munro, G. Holder, V. Plagnol, 2016, American journal of human genetics.

Jonathan E. Dickerson, S. Bhaskar, G. Hall, 2012, Journal of Medical Genetics.

Christopher Campbell, Rachel L. Taylor, Catriona Tate, 2017, Journal of Medical Genetics.

D. Mackey, R. Newbury-Ecob, A. Markham, 2001, Human molecular genetics.

J. Clayton-Smith, W. Dobyns, E. Sherr, 2010, American journal of medical genetics. Part A.

J. Shendure, H. Mefford, E. Zackai, 2011, American journal of medical genetics. Part A.

Stephanie Halford, Julius O. B. Jacobsen, Daniel Greene, 2017, Bioinform..

R. Hennekam, L. Biesecker, J. Graham, 2010, Human mutation.

J. Clayton-Smith, W. Newman, S. Bhaskar, 2021, Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery.

G. Hall, G. Black, R. Gillespie, 2014, Clinical & experimental ophthalmology.

D. Mackey, L. Kearns, S. Staffieri, 2012, Clinical & experimental ophthalmology.

W. Newman, G. Black, 2014, Genes.

Rachel L. Taylor, Mark T. Handley, J. Clayton-Smith, 2017, Investigative ophthalmology & visual science.

I. C. Lloyd, J. Clayton-Smith, S. Williams, 2016, Ophthalmology.

I. C. Lloyd, J. Lamb, S. Daiger, 2016, Journal of Medical Genetics.

G. Black, I. Bruce, L. Molina-Ramírez, 2020, Cochlear implants international.

Katherine R. Smith, J. Clayton-Smith, G. Hall, 2019, Scientific Reports.

B. Lorenz, D. Fischer, F. Parmeggiani, 2021, Orphanet Journal of Rare Diseases.

Rachel L. Taylor, S. Antonarakis, C. Pournaras, 2018, American journal of human genetics.

I. C. Lloyd, K E Chandler, J. Clayton-Smith, 2002, The British journal of ophthalmology.

Rachel L. Taylor, F. Brancati, U. Kornak, 2020, Clinical genetics.

William J. Astle, Sri V. V. Deevi, Kenneth G. C. Smith, 2020, Nature.

W. Newman, G. Black, J. Ellingford, 2021, eLife.

P. Sergouniotis, E. Lenassi, S. Ramsden, 2020, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

A. Wright, X. Shu, S. Ramsden, 2007, Human mutation.

J. Clayton-Smith, B. Kerr, S. Ramsden, 2001, Journal of medical genetics.

A. Webster, M. Seabra, S. Ramsden, 2013, European Journal of Human Genetics.

Rachel L. Taylor, E. Lenassi, S. Douzgou, 2019, European Journal of Human Genetics.

G. Hall, A. Webster, A. Moore, 2013, European journal of medical genetics.

R. Nash, A. Rajai, S. Saeed, 2022, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

G. Hall, G. Black, Eleanor McVeigh, 2019, Journal of Community Genetics.

G. Hall, K. Payne, A. Webster, 2013, European Journal of Human Genetics.

N. Parry, S. Kelly, G. Black, 2018, BMJ Case Reports.

Shalaw R. Sallah, S. Lovell, P. Sergouniotis, 2022, The Journal of molecular diagnostics : JMD.

Shalaw R. Sallah, S. Lovell, P. Sergouniotis, 2021, Journal of Medical Genetics.

A. Howell, D. Evans, W. Newman, 2009, Journal of Medical Genetics.

P. Sergouniotis, G. Black, A. Jalil, 2022, Retina.

Jennifer R. Davies, I. C. Lloyd, M. Votruba, 2014, neurogenetics.

Rachel L. Taylor, P. Pouwels, R. Houwen, 2018, Human molecular genetics.

G. Hall, G. Black, Eleanor McVeigh, 2019, Journal of Community Genetics.

Stephanie Halford, Julius O. B. Jacobsen, Susan M. Downes, 2016, bioRxiv.

R. Kaneva, A. Wright, S. Bhattacharya, 2006, Molecular vision.

E. Lenassi, G. Black, J. Ashworth, 2016, Acta ophthalmologica.

E. Birney, P. Sergouniotis, S. Javerzat, 2023, Journal of Medical Genetics.

J. Clayton-Smith, P. Sergouniotis, G. Black, 2023, Genes.

P. Sergouniotis, G. Black, J. Ellingford, 2017, Clinical & experimental ophthalmology.

G. Hall, G. Black, R. Gillespie, 2014, Clinical & experimental ophthalmology.

Anna Rudenko, Kanmin Xue, Susan M Downes, 2018, Nature Medicine.